Reducing Risks In Your SIP Validation Cycles

In Sterilize in Place (SIP) validation cycles, every detail is crucial. Every aspect, from the positioning to maintaining the integrity of biological indicators, must be precise; any deviation can result in erroneous outcomes and potential process risks. Numerous issues can be introduced by utilizing tape for positioning during SIP validation, ultimately undermining the process' validity. Continue reading to explore the top nine reasons why tape should not be relied upon during SIP validation cycles.